Related Experiment Video
Updated: Jul 24, 2025
A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
Published on: August 17, 2016
Replacing Oxygen Evolution with Hydrazine Borane Oxidation for Energy-Saving Electrochemical Hydrogen Production
Yefei Peng1, Minsong Huang1, Qifeng Yang2
1Key Laboratory of Energy Catalysis and Conversion of Nanchang, College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, China.
Abstract:
Electrochemical water splitting is a green strategy for hydrogen (H2) production but is severely hindered by the sluggish anodic oxygen evolution reaction (OER). Therefore, replacing the sluggish anodic OER with more favorable oxidation reactions is an energy-saving approach for hydrogen production. Hydrazine borane (HB, N2H4BH3) is considered a potential hydrogen storage material due to its easy preparation, nontoxicity, and high chemical stability. Furthermore, the complete electrooxidation of HB has a unique characteristic of a much lower potential compared to that of OER. All these make it an ideal alternative for energy-saving electrochemical hydrogen production, however, which has never been reported so far. Herein, HB oxidation (HBOR)-assisted overall water splitting (OWS) is proposed for the first time for energy-saving electrochemical hydrogen production. The as-synthesized NiCoP@CoFeP nanoneedle array catalyst exhibited superefficient OER, hydrogen evolution reaction (HER), and HBOR performance. Impressively, NiCoP@CoFeP serves as both anodic and cathodic electrocatalysts for HB-assisted OWS, only requires a low cell voltage of only 0.078 V to achieve a current density of 10 mA cm-2, which was 1.4 V lower than that for HB-free OWS, indicating the highly energy-saving H2 production.
Related Concept Videos
03:08Hydroboration-Oxidation of Alkenes
02:36Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
02:47Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
02:23Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
02:15Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
01:28Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation